Sydney School of Public Health, University of Sydney, Camperdown, New South Wales, Australia; Centre for Kidney Research at The Children's Hospital at Westmead, Sydney, New South Wales, Australia; Child and Adolescent Renal Service, Children's Health Queensland, Brisbane, Queensland, Australia.
Department of Nephrology, Princess Alexandra Hospital, Brisbane, Australia; Australasian Kidney Trials Network, Diamantina Institute, University of Queensland, Brisbane, Queensland, Australia; Translational Research Institute, Brisbane, Queensland, Australia.
Kidney Int. 2018 Oct;94(4):809-817. doi: 10.1016/j.kint.2018.06.009. Epub 2018 Aug 30.
Better prognostication of graft and patient outcomes among kidney transplant recipients with post-transplant lymphoproliferative disease (PTLD) in the rituximab era is needed to inform treatment decisions. Therefore, we sought to estimate the excess risks of death and graft loss in kidney transplant recipients with PTLD, and to determine risk factors for death. Using the ANZDATA registry, the risks of mortality and graft loss among recipients with and without PTLD were estimated using survival analysis. A group of 367 patients with PTLD (69% male, 85% white, mean age 43 years) were matched 1 to 4 to 1468 controls (69% male, 88% white, mean age 43 years), and followed for a mean of 16 years. Recipients with PTLD experienced poorer 10-year patient survival (41%, 95% confidence intervals 36-47%) than controls (65%, 63-68%). Excess mortality occurred in the first 2 years post-transplant (hazard ratio 8.5, 6.7-11), but not thereafter (1.0, 0.76-1.3). Cerebral lymphoma (2.0, 1.3-3.1), bone marrow disease (2.0, 1.2-3.3) and year of diagnosis prior to 2000 (2.2, 1.4-3.5; after 2000 reference) were risk factors of death. PTLD did not confer an excess risk of graft loss (1.08, 0.69-1.70). Thus, PTLD is a risk factor for death, particularly in the first two years after diagnosis. Cerebral or bone marrow diseases were associated with increased mortality risk, but overall survival in the rituximab era (post 2000) has improved.
在利妥昔单抗时代,需要更好地预测移植后淋巴组织增生性疾病(PTLD)的肾移植受者的移植物和患者结局,以告知治疗决策。因此,我们试图估计 PTLD 肾移植受者死亡和移植物丢失的超额风险,并确定死亡的危险因素。我们使用 ANZDATA 登记处,通过生存分析估计了 PTLD 受者和无 PTLD 受者的死亡率和移植物丢失率。一组 367 例 PTLD 患者(69%为男性,85%为白人,平均年龄为 43 岁)与 1468 例对照(69%为男性,88%为白人,平均年龄为 43 岁)进行 1:4 配对,平均随访 16 年。PTLD 受者 10 年患者生存率(41%,95%置信区间 36-47%)低于对照组(65%,63-68%)。移植后 2 年内发生超额死亡率(危险比 8.5,6.7-11),但此后不再发生(1.0,0.76-1.3)。脑淋巴瘤(2.0,1.3-3.1)、骨髓疾病(2.0,1.2-3.3)和 2000 年前诊断的年份(2.2,1.4-3.5;2000 年后为参考)是死亡的危险因素。PTLD 并未增加移植物丢失的风险(1.08,0.69-1.70)。因此,PTLD 是死亡的危险因素,特别是在诊断后的前两年。脑或骨髓疾病与死亡率增加相关,但利妥昔单抗时代(2000 年后)的总体生存率有所提高。